Merck
All Photos(2)

D146005

Sigma-Aldrich

2,6-Dimethylaniline

99%

Synonym(s):
2,6-Xylidine, 2-Amino-1,3-dimethylbenzene, 2-Amino-m-xylene
Linear Formula:
(CH3)2C6H3NH2
Molecular Weight:
121.18
Beilstein:
636332
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

<0.01 mmHg ( 20 °C)

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.560 (lit.)

bp

214 °C/739 mmHg (lit.)

mp

10-12 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(C)c1N

InChI

1S/C8H11N/c1-6-4-3-5-7(2)8(6)9/h3-5H,9H2,1-2H3

InChI key

UFFBMTHBGFGIHF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
44232736766PHR1669
2,6-Dimethylaniline 99%

Sigma-Aldrich

D146005

2,6-Dimethylaniline

2,6-Dimethylaniline analytical standard

Supelco

442327

2,6-Dimethylaniline

2,6-Dimethylaniline PESTANAL&#174;, analytical standard

Supelco

36766

2,6-Dimethylaniline

form

liquid

form

-

form

-

form

-

refractive index

n20/D 1.560 (lit.)

refractive index

n20/D 1.560 (lit.)

refractive index

n20/D 1.560 (lit.)

refractive index

n20/D 1.560 (lit.)

bp

214 °C/739 mmHg (lit.)

bp

214 °C/739 mmHg (lit.)

bp

214 °C/739 mmHg (lit.)

bp

214 °C/739 mmHg (lit.)

mp

10-12 °C (lit.)

mp

10-12 °C (lit.)

mp

10-12 °C (lit.)

mp

10-12 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

Application

2,6-Dimethylaniline can react with:
  • 1-Naphthaldehyde to form an intermediate, bis(4-amino-3,5-dimethylphenyl)naphthylmethane (BADN) to further form bis(4-maleimido-3,5-dimethylphenyl)naphthylmethane (BMDN) by reacting with maleic anhydride, acetic anhydride and sodium acetate.
  • n-Butyllithium to form lithium 2,6-dimethylanilide, which can be utilized to form various RhII anilide complexes.

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Documents related to the products that you have purchased in the past have been gathered in the Document Library for your convenience.

Visit the Document Library

Difficulty Finding Your Product Or Lot/Batch Number?

Product numbers are combined with Pack Sizes/Quantity when displayed on the website (example: T1503-25G). Please make sure you enter ONLY the product number in the Product Number field (Example: T1503).

Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

Having trouble? Feel free to contact Technical Service for assistance.

Lot and Batch Numbers can be found on a product's label following the words 'Lot' or 'Batch'.

Aldrich Products

  • For a lot number such as TO09019TO, enter it as 09019TO (without the first two letters 'TO').

  • For a lot number with a filling-code such as 05427ES-021, enter it as 05427ES (without the filling-code '-021').

  • For a lot number with a filling-code such as STBB0728K9, enter it as STBB0728 without the filling-code 'K9'.

Not Finding What You Are Looking For?

In some cases, a COA may not be available online. If your search was unable to find the COA you can request one.

Request COA

Customers Also Viewed

Slide 1 of 8

1 of 8

2,5-Dimethylaniline 99%

Sigma-Aldrich

102253

2,5-Dimethylaniline

Bupivacaine impurity F European Pharmacopoeia (EP) Reference Standard

Y0001575

Bupivacaine impurity F

2,4-Dimethylaniline &#8805;99%

Sigma-Aldrich

240915

2,4-Dimethylaniline

N,N-Dimethylaniline ReagentPlus&#174;, 99%

Sigma-Aldrich

515124

N,N-Dimethylaniline

2,3-Dimethylaniline 99%

Sigma-Aldrich

D145807

2,3-Dimethylaniline

Reactivity of Rhodium (II) Amido/Rhodium (I) Aminyl Complexes
Zhang N, et al.
Inorgorganica Chimica Acta, 39(13), 2921-2927 (2018)
Novel bismaleimide with naphthalene side group. 1. From 1-naphthaldehyde and 2, 6-dimethylaniline
Wang CS, et al.
Polymer, 39(13), 2921-2927 (1998)
Kai Cheng et al.
Royal Society open science, 6(6), 190196-190196 (2019-07-18)
A novel aromatic diamine containing pyridyl side group, 4-pyridine-4,4-bis(3,5-dimethyl-5-aminophenyl)methane (PyDPM), was successfully synthesized via electrophilic substitution reaction. The polyimides (PIs) containing pyridine were obtained via the microwave-assisted one-step polycondensation of the PyDPM with pyromellitic dianhydride (PMDA), 3,3',4,4'-biphenyltetracarboxylic dianhydride (BPDA), 3,3',4,4'-diphenylether
Nonglak Boonrattanakij et al.
Journal of hazardous materials, 172(2-3), 952-957 (2009-08-21)
This research investigated the intrinsic second-order rate constant between 2,6-dimethyl-aniline (2,6-DMA) and hydroxyl radicals (OH) using Fenton's reactions under both batch and continuous operations. The competitive kinetics technique with aniline as a reference compound was employed. In the batch study
Wang-Ping Ting et al.
Journal of hazardous materials, 161(2-3), 1484-1490 (2008-06-17)
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed to degrade organic toxic contaminants. The use of UVA light and electric current as electron donors can efficiently initiate the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service